ClinVar Genomic variation as it relates to human health
GRCh38/hg38 13q33.2(chr13:105209681-105727745)x1
Germline
Classification
(1)
Uncertain significance
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
DAOA | - | - |
GRCh38 GRCh37 |
- | 128 | |
DAOA-AS1 | - | - |
GRCh38 GRCh37 |
- | 128 | |
LINC00343 | - | - | - | GRCh38 | - | 41 |
LOC110120930 | - | - | - | GRCh38 | - | 39 |
LOC126861836 | - | - | - | GRCh38 | - | 39 |
LOC132090155 | - | - | - | GRCh38 | - | 40 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
See cases
|
Uncertain significance (1) |
|
Aug 12, 2011 | RCV000050909.6 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 08, 2024